SCOPUS 정보 검색 플랫폼

Volumn 116, Issue 5, 2005, Pages 416-419

Molecular analysis of congenital scoliosis: A candidate gene approach

(9) Maisenbacher, Melissa K a Han, Ji Soo a O'Brien, Megan L a Tracy, Michael R a Erol, Bülent a Schaffer, Alyssa A a Dormans, John P b Zackai, Elaine H a,b Kusumi, Kenro a,b

a CHILDREN S HOSPITAL OF PHILADELPHIA (United States)

b UNIVERSITY OF PENNSYLVANIA (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CONGENITAL HEART MALFORMATION; CONGENITAL SCOLIOSIS; DELTA LIKE 3 GENE; FAMILIAL DISEASE; GENE; HUMAN; IDIOPATHIC SCOLIOSIS; INCIDENCE; KIDNEY ANOMALY; MISSENSE MUTATION; NONHUMAN; PRIORITY JOURNAL; SCOLIOSIS;

ABNORMALITIES, MULTIPLE; COHORT STUDIES; HUMANS; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; MEMBRANE PROTEINS; MUTATION; SCOLIOSIS; SYNDROME;

EID: 17144382468 PISSN: 03406717 EISSN: None Source Type: Journal
DOI: 10.1007/s00439-005-1253-8 Document Type: Article

Times cited : (49)

References (6)

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2
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3
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- Congenital scoliois
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6
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.